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Targeting mutant p53 in cancer: the latest insights

This commentary wishes to highlight the latest discoveries in the mutant p53 field that have been discussed in the 8th p53 Mutant Workshop 2019, held in Lyon. TP53 mutant (mutp53) proteins are involved in the pathogenesis of most human cancers. Mutp53 proteins not only lose wild-typ53 function but,...

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Autores principales: Di Agostino, Silvia, Fontemaggi, Giulia, Strano, Sabrina, Blandino, Giovanni, D’Orazi, Gabriella
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612074/
https://www.ncbi.nlm.nih.gov/pubmed/31277687
http://dx.doi.org/10.1186/s13046-019-1302-0
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author Di Agostino, Silvia
Fontemaggi, Giulia
Strano, Sabrina
Blandino, Giovanni
D’Orazi, Gabriella
author_facet Di Agostino, Silvia
Fontemaggi, Giulia
Strano, Sabrina
Blandino, Giovanni
D’Orazi, Gabriella
author_sort Di Agostino, Silvia
collection PubMed
description This commentary wishes to highlight the latest discoveries in the mutant p53 field that have been discussed in the 8th p53 Mutant Workshop 2019, held in Lyon. TP53 mutant (mutp53) proteins are involved in the pathogenesis of most human cancers. Mutp53 proteins not only lose wild-typ53 function but, in some circumstances, may acquire novel oncogenic functions, namely gain-of-function (GOF), which lead to aberrant cell proliferation, chemoresistance, disruption of tissue architecture, migration, invasion and metastasis. Decoding the TP53 mutational spectrum and mutp53 interaction with additional transcription factors will therefore help to developing and testing novel and hopefully more efficient combinatorial therapeutic approaches.
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spelling pubmed-66120742019-07-16 Targeting mutant p53 in cancer: the latest insights Di Agostino, Silvia Fontemaggi, Giulia Strano, Sabrina Blandino, Giovanni D’Orazi, Gabriella J Exp Clin Cancer Res Commentary This commentary wishes to highlight the latest discoveries in the mutant p53 field that have been discussed in the 8th p53 Mutant Workshop 2019, held in Lyon. TP53 mutant (mutp53) proteins are involved in the pathogenesis of most human cancers. Mutp53 proteins not only lose wild-typ53 function but, in some circumstances, may acquire novel oncogenic functions, namely gain-of-function (GOF), which lead to aberrant cell proliferation, chemoresistance, disruption of tissue architecture, migration, invasion and metastasis. Decoding the TP53 mutational spectrum and mutp53 interaction with additional transcription factors will therefore help to developing and testing novel and hopefully more efficient combinatorial therapeutic approaches. BioMed Central 2019-07-05 /pmc/articles/PMC6612074/ /pubmed/31277687 http://dx.doi.org/10.1186/s13046-019-1302-0 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Commentary
Di Agostino, Silvia
Fontemaggi, Giulia
Strano, Sabrina
Blandino, Giovanni
D’Orazi, Gabriella
Targeting mutant p53 in cancer: the latest insights
title Targeting mutant p53 in cancer: the latest insights
title_full Targeting mutant p53 in cancer: the latest insights
title_fullStr Targeting mutant p53 in cancer: the latest insights
title_full_unstemmed Targeting mutant p53 in cancer: the latest insights
title_short Targeting mutant p53 in cancer: the latest insights
title_sort targeting mutant p53 in cancer: the latest insights
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6612074/
https://www.ncbi.nlm.nih.gov/pubmed/31277687
http://dx.doi.org/10.1186/s13046-019-1302-0
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